1. Some quantitative uses of drug antagonists;Arunlakshana;Br. J. Pharmacol.,1959
2. (+)-Niguldipine binds with very high affinity to Ca2+ channels and to a subtype of α1-adrenergic receptors;Boer;Eur. J. Pharmacol.,1989
3. Ca2+ utilization in the constriction of rat aorta to full and partial alpha-1 adrenoceptor agonists;Chiu;J. Pharmacol. Exp. Ther.,1986
4. Relationship between phosphatidylinositol turnover and Ca++ mobilization induced by alpha-1 adrenoceptor stimulation in the rat aorta;Chiu;J. Pharmacol. Exp. Ther.,1987
5. Molecular cloning and expression of the cDNA for the hamster α1-adrenergic receptor;Cotecchia,1988